Domain 4Healthcare Access
Access is more than a clinic existing.
In this research, access refers to both timely diagnosis and timely entry into therapeutic care during the early childhood window. Families often wait 6–12 months for evaluations (Williams et al., 2021), and many children are not diagnosed until age 5 or later, even though autism can be reliably identified as early as 18 months. The time between a parent’s first concern and a formal diagnosis can stretch from 12 to 55 months, showing how quickly “early identification” can become years of waiting in real life (Makino et al., 2021; Buffle et al., 2025). Families often must consult three to five professionals before their child is diagnosed (Isaac et al., 2025).
These diagnostic delays often continue after diagnosis, as families face additional waitlists for services such as OT, PT, ST, ABA, infant stimulation, and developmental supports. In this way, delays compound across the early intervention window: from concern, to evaluation, to diagnosis, to actual therapeutic care.
Access is also shaped by disparities within disparities. Wait times and care pathways may differ by socioeconomic status, race, ethnicity, language, geography, insurance type, gender, and caregiver capacity to advocate and navigate fragmented systems. For many families, access is not simply whether a service exists. It is whether the right service is available, affordable, culturally responsive, clinically appropriate, and reachable when the child needs it most.
WAIT TIMESDISPARITIESINSURANCE BARRIERSQUALITY